IMPORTANCE OF TURBIDITY
7.1 Overview
Section 2 of this guidance manual is included to present an overview on the definition and
sources of turbidity. Understanding turbidity, its causes and sources, and the significance
to human health will provide the background on which the new turbidity standards are
based.
• Waste discharges;
• Runoff from watersheds, especially those that are disturbed or eroding;
• Algae or aquatic weeds and products of their breakdown in water reservoirs,
rivers, or lakes;
• Humic acids and other organic compounds resulting from decay of plants,
leaves, etc. in water sources; and
• High iron concentrations which give waters a rust-red coloration (mainly in
ground water and ground water under the direct influence of surface water).
• Air bubbles and particles from the treatment process (e.g., hydroxides, lime
softening)
Simply stated, turbidity is the measure of relative clarity of a liquid. Clarity is important
when producing drinking water for human consumption and in many manufacturing uses.
Once considered as a mostly aesthetic characteristic of drinking water, significant evidence
exists that controlling turbidity is a competent safeguard against pathogens in drinking
water.
The first practical attempts to quantify turbidity date to 1900 when Whipple and Jackson
developed a standard suspension fluid using 1,000 parts per million (ppm) of
diatomaceous earth in distilled water (Sadar, 1996). Dilution of this reference suspension
resulted in a series of standard suspensions, which were then used to derive a ppm-silica
scale for calibrating turbidimeters.
The standard method for determination of turbidity is based on the Jackson candle
turbidimeter, an application of Whipple and Jackson's ppm-silica scale (Sadar, 1996). The
Jackson candle turbidimeter consists of a special candle and a flat-bottomed glass tube
(Figure 7-2), and was calibrated by Jackson in graduations equivalent to ppm of
suspended silica turbidity. A water sample is poured into the tube until the visual image of
the candle flame, as viewed from the top of the tube, is diffused to a uniform glow. When
the intensity of the scattered light equals that of the transmitted light, the image
disappears; the depth of the sample in the tube is read against the ppm-silica scale, and
turbidity was measured in Jackson turbidity units (JTU). Standards were prepared from
materials found in nature, such as Fuller's earth, kaolin, and bed sediment, making
consistency in formulation difficult to achieve.
Eye
Scattered Light is as
Intense as Transmitted
Light-Image of Flame
Disappears at this Depth
Scattered Light
Length of Arrow
Proportional to Intensity
of Beam of Light
Even though the consistency of formazin improved the accuracy of the Jackson Candle
Turbidimeter, it was still limited in its ability to measure extremely high or low turbidity.
More precise measurements of very low turbidity were needed to define turbidity in
samples containing fine solids. The Jackson Candle Turbidimeter is impractical for this
because the lowest turbidity value on this instrument is 25 JTU. The method is also
cumbersome and too dependent on human judgement to determine the exact extinction
point.
Finally, turbidity measurement standards changed in the 1970's when the nephelometric
turbidimeter, or nephelometer, was developed which determines turbidity by the light
scattered at an angle of 90E from the incident beam (Figure 7-3). A 90E detection angle is
considered to be the least sensitive to variations in particle size. Nephelometry has been
adopted by Standard Methods as the preferred means for measuring turbidity because of
the method's sensitivity, precision, and applicability over a wide range of particle size and
concentration. The nephelometric method is calibrated using suspensions of formazin
polymer such that a value of 40 nephelometric units (NTU) is approximately equal to 40
JTU (AWWARF, 1998). The preferred expression of turbidity is NTU.
Glass
Sample Cell
Transmitted
Light
90°° Scattered
Light
Lamp Lens Aperture
Detector
The particles of turbidity provide “shelter” for microbes by reducing their exposure to
attack by disinfectants (Figure 7-4). Microbial attachment to particulate material or inert
substances in water systems has been documented by several investigators (Marshall,
1976; Olson et al., 1981; Herson et al., 1984) and has been considered to aid in microbe
survival (NAS, 1980). Fortunately, traditional water treatment processes have the ability
to effectively remove turbidity when operated properly.
Protected
Micro-organisms
Exposed
Micro-organisms
Particulates
Giardia and Cryptosporidium are the two most studied organisms known to cause
waterborne illnesses. These two protozoa are believed to be ubiquitous in source water,
are known to occur in drinking water systems, have been responsible for the majority of
waterborne outbreaks, and treatments to remove and/or inactivate them are known to be
effective for a wide range of waterborne parasites (LeChevallier and Norton, in Craun,
1993). Giardia and Cryptosporidium have caused over 400,000 persons in the United
States to become ill since 1991, mostly due to a 1993 outbreak in Milwaukee, Wisconsin.
Giardia and viruses are addressed under the 1989 SWTR. Systems using surface water
must provide adequate treatment to remove and/or inactivate at least 3-log (99.9%) of the
Giardia lamblia cysts and at least 4-log (99.99%) of the enteric viruses. However,
Cryptosporidium was not addressed in the SWTR due to lack of occurrence and health
effects data. In the mid-1980's, the United States experienced its first recognized
waterborne disease outbreak of cryptosporidiosis (D'Antonio et al., 1985). It was soon
discovered that the presence of Cryptosporidium in drinking water, even in very low
As an example, data gathered by LeChevallier and Norton (in Craun, 1993) from three
drinking water treatment plants using different watersheds indicated that for every log
removal of turbidity, 0.89 log removal was achieved for the parasites Cryptosporidium
and Giardia (Figures 7-5 and 7-6). Of course, this exact relationship does not hold for all
treatment plants. Table 7-2 lists several other studies in addition to LeChevallier and
Norton's, and their conclusions on the relationship of turbidity to protozoan removal.
All studies in Table 7-2 show turbidity as a useful predictor of parasite removal efficiency.
This evidence suggests that although a very low turbidity value does not completely
ensure that particles are absent, it is an excellent measure of plant optimization to ensure
maximum public health protection.
5
logY = 0.892(logx) + 0.694
4
Log Removal Giardia
r = 0.780
3
-1
-1.0 0.0 1.0 2.0 3.0 4.0
Log Removal Turbidity
Source: LeChevallier and Norton, 1991.
3.0
logY = 0.996(logx) + 0.494
2.1 r = 0.771
1.1
0.1
-0.9
7.4 References
1. Anderson, W.L., et al. 1996. “Biological Particle Surrogates for Filtration
Performance Evaluation.”
2. CDC (Centers for Disease Control). 1996. “Surveillance for Waterborne-Disease
Outbreaks - United States, 1993-1994.” Morbidity and Mortality Weekly Report,
45(SS-1).
3. D'Antonio, R.G., R.E. Winn, J.P. Taylor, et al. 1985. “A Waterborne Outbreak of
Cryptosporidiosis in Normal Hosts.” Annals of Internal Medicine. 103:886-888.
4. Fox, K.R. 1995. “Turbidity as it relates to Waterborne Disease Outbreaks.”
Presentation at M/DBP Information Exchange, Cincinnati, Ohio. AWWA white
paper.
5. Gregory, J. 1994. “Cryptosporidium in Water: Treatment and Monitoring
Methods.” Filtration & Separation. 31:283-289.
6. Hall, T., J. Presdee, and E. Carrington. 1994. “Removal of Cryptosporidium oocysts
by water treatment processes.” Foundation for Water Research.
7. Herson, D.S., D.R. Marshall, and H.T. Victoreen. 1984. “Bacterial persistence in
the distribution system.” J. AWWA. 76:309-22.
8. LeChevallier, M.W., W.D. Norton, and R.G. Lee. 1991. “Giardia and
Cryptosporidium in Filtered Drinking Water Supplies.” Applied and Environmental
Microbiology. 2617-2621.
9. LeChevallier, M.W. and W.D. Norton. 1992. “Examining Relationships Between
Particle Counts and Giardia, Cryptosporidium, and Turbidity.” J. AWWA.
10. LeChevallier, M.W. and W.D. Norton. “Treatments to Address Source Water
Concerns: Protozoa.” Safety of Water Disinfection: Balancing Chemical and
Microbial Risks. G.F. Craun, editor. ILSI Press, Washington, D.C.
11. Marshall, K.C. 1976. Interfaces in microbial ecology. Harvard University Press,
Cambridge, MA.
12. NAS (National Academy of Sciences). 1980. National Research Council: drinking
water and health, Volume 2. National Academy Press, Washington, D.C.
13. Nieminski, E.C. 1992. “Giardia and Cryptosporidium - Where do the cysts go.”
Conference proceedings, AWWA Water Quality Technology Conference.
14. Olson, B.H., H.F. Ridgway, and E.G. Means. 1981. “Bacterial colonization of
mortar-lined and galvanized iron water distribution mains.” Conference proceedings,
AWWA National Conference. Denver, CO.
15. Ongerth, J.E. 1990. “Evaluation of Treatment for Removing Giardia Cysts.” J.
AWWA. 82(6):85-96.
16. Sadar, M.J. 1996. Understanding Turbidity Science. Hach Company Technical
Information Series - Booklet No. 11.
17. USEPA. 1997. Occurrence Assessment for the Interim Enhanced Surface Water
Treatment Rule, Final Draft. Office of Ground Water and Drinking Water,
Washington, D.C.
18. USEPA. 1983. Turbidity Removal for Small Public Water Systems. Office of
Ground Water and Drinking Water, Washington, D.C.
7. IMPORTANCE OF TURBIDITY........................................................................................................7-1
7.1 OVERVIEW.............................................................................................................................................7-1
7.2 TURBIDITY: DEFINITION, CAUSES, AND HISTORY AS A WATER QUALITY PARAMETER .....................7-1
7.3 TURBIDITY'S SIGNIFICANCE TO HUMAN HEALTH ................................................................................7-4
7.3.1 Waterborne Disease Outbreaks..................................................................................................7-5
7.3.2 The Relationship Between Turbidity Removal and Pathogen Removal....................................7-7
7.4 REFERENCES .......................................................................................................................................7-10